82-45-1

  • Product Name:1-Aminoanthraquinone
  • Molecular Formula:C14H9NO2
  • Purity:99%
  • Molecular Weight:223.231
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Product Details;

CasNo: 82-45-1

Molecular Formula: C14H9NO2

Appearance: deep brown crystalline powder

Chinese Manufacturer Supply Top Purity 1-Aminoanthraquinone 82-45-1 with Low Price

  • Molecular Formula:C14H9NO2
  • Molecular Weight:223.231
  • Appearance/Colour:deep brown crystalline powder 
  • Vapor Pressure:8.04E-09mmHg at 25°C 
  • Melting Point:253-255 °C(lit.) 
  • Refractive Index:1.707 
  • Boiling Point:464.9 °C at 760 mmHg 
  • PKA:-0.51±0.20(Predicted) 
  • Flash Point:235 °C 
  • PSA:60.16000 
  • Density:1.383 g/cm3 
  • LogP:2.62540 

1-Amino anthraquinone(Cas 82-45-1) Usage

Description

1-Amino anthraquinone is a chemical compound that plays a crucial role in the synthesis of anthraquinone dyes, which are a significant class of dyes used in various industries, particularly the textile and dyeing industry.

Chemical Properties

deep brown crystalline powder

Uses

1-Amino anthraquinone is a fundamental raw material for the production of various types of dyes, including acid dyes, reactive dyes, disperse dyes, and vat dyes. It is essential in the synthesis of these dyes and contributes to the coloration of fabrics and other materials.

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C14H9NO2/c15-11-7-3-6-10-12(11)14(17)9-5-2-1-4-8(9)13(10)16/h1-7H,15H2

82-45-1 Relevant articles

1-Aminoanthraquinone derivatives as a novel corrosion inhibitor for carbon steel API 5L-X60 in white petrol–water mixtures

N. Muthukumar a c, A. Ilangovan b, S. Maruthamuthu a, N. Palaniswamy a, A. Kimura c

, Materials Chemistry and Physics Volume 115, Issue 1, 15 May 2009, Pages 444-452

Oleic acid derivative of 1-aminoanthraquinone was found to be the best corrosion inhibitor. It exhibited 86% inhibition efficiency against the corrosion of API 5L-X60 steel.

Copper-catalyzed one-pot relay synthesis of anthraquinone based pyrimidine derivative as a probe for antioxidant and antidiabetic activity

Ahmad, Zaheer,Arshad, Uzma,Parveen, Shagufta,Rafiq, Naila,Shafiq, Nusrat,Zarren, Gul

, (2020/12/17)

Synthetic compounds have modernized the ...

Intramolecular Hydrogen Bonding in 1,8-Dihydroxyanthraquinone, 1-Aminoanthraquinone, and 9-Hydroxyphenalenone Studied by Picosecond Time-Resolved Fluorescence Spectroscopy in a Supersonic Jet†

Christian Müller, Jörg Schroeder, and Jürgen Troe

, J. Phys. Chem. B 2006, 110, 40, 19820–19832

We investigated spectroscopic and dynamic fluorescence properties of the S1 ← S0 transitions of three intramolecularly hydrogen-bonded molecules, 1,8-dihydroxyanthraquinone (1,8-DHAQ), 1-aminoanthraquinone (1-AAQ), and 9-hydroxyphenalenone (9-HPA), by determining their fluorescence excitation spectra and state-selective fluorescence lifetimes under supersonic jet conditions.

82-45-1 Process route

1-nitroanthraquinone
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1-nitroanthraquinone

1,1'-(1,2-ethanediyl)bisbenzene
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1,1'-(1,2-ethanediyl)bisbenzene

1-amino-9,10-anthracenedione
82-45-1

1-amino-9,10-anthracenedione

benzaldehyde
100-52-7

benzaldehyde

Conditions
Conditions Yield
 
 
reactive blue 19
2580-78-1

reactive blue 19

3-aminophthalic acid
5434-20-8,857040-74-5

3-aminophthalic acid

1,4-dihydroxy-9,10-anthracenedione
81-64-1,103220-12-8

1,4-dihydroxy-9,10-anthracenedione

1,4-diamino-9,10-dioxo-9,10-dihydro-anthracene-2-sulfonic acid
4095-85-6

1,4-diamino-9,10-dioxo-9,10-dihydro-anthracene-2-sulfonic acid

1-amino-9,10-anthracenedione
82-45-1

1-amino-9,10-anthracenedione

benzene-1,2-dicarboxylic acid
88-99-3,73607-73-5

benzene-1,2-dicarboxylic acid

Conditions
Conditions Yield
With chitosan/polyaniline/CdS nanocomposite; for 2h; pH=6; pH-value; Catalytic behavior; Kinetics; Irradiation;
 

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